检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:陈海滨[1] 黄琳[1] 黄清育[1] 凌雪萍[1,2] 朱锋[1] 黄河清[1,3,2]
机构地区:[1]厦门大学生命科学学院生物化学与生物技术学系,厦门361005 [2]厦门大学化学化工学院化学生物学系,厦门361005 [3]厦门大学海洋与环境科学学院近海海洋科学国家重点实验室,厦门361005
出 处:《分析化学》2009年第6期801-805,共5页Chinese Journal of Analytical Chemistry
基 金:国家自然科学基金项目(No.40776060);福建省高校创新研究团队基金资助
摘 要:比较丙酮/TCA沉淀法和直接裂解法,优化提取与分离褐云玛瑙螺(Achatina fulica,AF)肝脏全蛋白。采用丙酮/TCA沉淀法,可获得约600个蛋白质斑点。用0.5 mg/L CdCl2溶液浸泡后的去梗小白菜喂养AF,并作为镉盐诱导AF肝脏表达应激蛋白质的实验材料。采用蛋白质组学技术筛选出由镉盐诱导AF肝脏表达的14个差异蛋白质斑点,并用肽质量指纹图谱技术(peptide mass fingerprinting,PMF)和数据库比对法初步鉴定出7种差异蛋白质,其中部分为热激蛋白(heat shock protein)、甲基转移酶(Methyltransferase)、三磷酸腺苷结合盒子转运体(ABC transporter)、钼酸盐转运子亚基(molybdate transporter subunit)和磷酸甘油酸变位酶(phosphoglycerate mutase)。差异蛋白质均参与镉盐代谢,并适合作为监测土壤或食物中镉污染程度及危害性的指示蛋白质。In comparison with direct lysis, the precipitation analysis of acetone/trichloroacetic acid was selected to optimize and separate whole proteins from the liver tissue of Achatina fulica(AF). By this method, approximately 600 protein spots in gel were obtained. Using a cabbage exposed by 0.05 mg/L CdCl2 as AF food, the liver was selected to reveal the stress proteins in the AF exposed to acute cadmium toxicity. Fourteen of differential protein spots in AF liver were obtained by proteomics, and then seven of these spots were further identified by both peptide mass fingerprint(PMF) and database search, which indicated that these proteins in part were identified to be heat shock protein, methyhransferase, adenosine triphosphate binding cassette (ABC) transporter, molybdate transporter subunit, and phosphoglycerate mutase. The results suggest that these significant proteins can be connected with metabolism pathway of cadmium, and with biomarkers for monitoring the contamination level of the cadmium and evaluating the crisis level both food and soil.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.15